Identification of Berberine as a Novel Agonist of Fatty Acid Receptor GPR40

被引:19
|
作者
Rayasam, Geetha Vani [1 ]
Tulasi, Vamshi Krishna [1 ]
Sundaram, Sindhuja [1 ]
Singh, Winny [1 ]
Kant, Rajiv [1 ]
Davis, Joseph Alex [1 ]
Saini, Kulvinder Singh [1 ]
Ray, Abhijit [1 ]
机构
[1] Novel Drug Discovery Res R&D III RANBAXY, Dept Pharmacol, Gurgaon, Haryana, India
关键词
insulin; secretion; calcium; mobilization; diabetes; INDUCED DIABETIC-RATS; INSULIN-SECRETION; BETA-CELLS; ALLOXAN; DIET;
D O I
10.1002/ptr.3165
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Several herbal plants such as Chinese herb Rhizoma Coptidis have been reported to possess antidiabetic activity. Berberine is its major active constituent and functions as an insulin sensitizer and insulin secretagogue. It has been reported to modulate several signaling pathways and targets. The objective of the current study is to investigate if berberine can function as a ligand of fatty acid receptor GPR40, which stimulates glucose dependent insulin secretion. Towards this objective, a mammalian cell line with stable overexpression of GPR40 was generated and characterized. Berberine stimulated calcium mobilization with an EC50 of 0.76 mu M in this GPR40 overexpressing cell line. Further, berberine stimulated glucose dependent insulin secretion from rat pancreatic beta cell line. This suggests that berberine functions as an agonist of fatty acid receptor GPR40 and might be a novel antidiabetic mechanism of action for berberine. Copyright (C) 2010 John Wiley & Sons, Ltd.
引用
收藏
页码:1260 / 1263
页数:4
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